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Table 3 Genetic models analyses of the association between three SNPs and MI susceptibility

From: The association of functional polymorphisms in genes expressed in endothelial cells and smooth muscle cells with the myocardial infarction

SNP/group

Genotype

χ2

p

OR (95% CI)

rs1867624

Dominant

TT + CT

CC

   

Case

161 (0.40)

240 (0.60)

1.71

0.192

1.21 (0.91–1.61)

Control

146 (0.36)

263 (0.64)

  

Recessive

TT

CT + CC

   

Case

28 (0.07)

373 (0.93)

2.52

0.112

1.63 (0.89–2.98)

Control

18 (0.04)

391 (0.96)

  

rs2057482

Dominant

TT + CT

CC

   

Case

149 (0.37)

252 (0.63)

0.52

0.47

1.11 (0.83–1.48)

Control

142 (0.35)

267 (0.65)

   

Recessive

TT

CT + CC

   

Case

17 (0.04)

384 (0.96)

0.57

0.45

0.78 (0.41–1.49)

Control

22 (0.05)

387 (0.95)

   

rs3739998

Dominant

CC + GC

GG

   

Case

152 (0.38)

249 (0.62)

0.13

0.722

0.95 (0.71–1.26)

Control

160 (0.39)

249 (0.61)

  

Recessive

CC

GC + GG

   

Case

20 (0.05)

381 (0.95)

0.31

0.580

0.84 (0.46–1.55)

Control

24 (0.06)

385 (0.94)

  
  1. SNP single nucleotide polymorphism, MI myocardial infarction